I am tempted to start this entry with one of the numerous bureaucrat/light bulb jokes but add a European twist that whatever the number they first need to define what a light bulb is.
Unfortunately, this is no joke. After some years of trying to arrive at an “applicable” definition for nanotechnology as opposed to a “working” definition, the European Commission is still not ready to settle on one.
After sending out their draft definition for public input last year, the coordinator of the commission charged with developing the definition, Henrik Laursen feels the matter is still unsettled.
“It is clear that at a certain level many stakeholders are saying different things, and there is no absolute scientific definition,” Laursen commented.The hesitance to settle on a definition is due to the fact that whatever is finally arrived at will immediately dictate policy. The idea being that it’s better to get it right from the beginning rather than potentially screw up the development of nanotechnology products or risk human health and the environment with a regulatory framework built around a faulty definition. “We still have some decisions to take but what we will come up with eventually will not be a working definition, it will be a definition that will be applicable,” Laursen is quoted as saying. “There is no room for us to introduce a definition by trial and error, we are expected to make sure we act and we need to come up with something.” On the one hand, the European Chemical Industry Council (Cefic) is in favor of a weight-based definition since “”Weight is generally used in all chemical legislation and test procedures…” and on the other EU’s scientific committee on emerging and newly identified health risks (SCENIHR) argues that “the potential hazards of using these particles relates to the number of them within a particular product.” If I were to flip a coin, it appears it’s going to go in the direction of number of nanoparticles. But if we take the old toxicity formula Hazard x Exposure = Risk, it’s hard to see where “exposure” is represented in this definition.
It makes the approach of the US Food & Drug Administration as outlined by Carlos Peña, director of emerging technology programmes of the FDA, seem not only more workable but more effective. Peña explains that instead of focusing on a definition of nanotechnology, the FDA is instead investigating how nanoparticles and materials are being used in different sectors and making sure that the regulations for those sectors (i.e. food, drugs and cosmetics) are adequate to address their introduction.
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